ORPHA:75508
Angioosteohypotrophic syndrome
inactive · moved to ORPHA:217008Segmental venous malformation
Synonyms: Phlebectatic osteohypoplastic angiodysplasia · Servelle-Martorell syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Segmental venous malformation
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Angioosteohypotrophic syndrome | Phlebectatic osteohypoplastic angiodysplasia · Servelle-Martorell syndrome |
| fr | Syndrome angio-ostéo-hypotrophique | Syndrome de Servelle-Martorell |
| de | Angio-osteo-hypotrophisches Syndrom | Angiodysplasie, osteohypoplastische phlebektatische · Servelle-Martorell-Syndrom |
| es | Síndrome angio-osteo-hipotrófico | Síndrome de Servelle-Martorell |
| it | Sindrome angio-osteoipotrofica | Angiodisplasia osteo-ipoplasica flebectasica · Sindrome di Servelle-Martorell |
| nl | Angio-osteohypotrofisch syndroom | Flebectatische osteohypoplastische angiodysplasie · Syndroom van Servelle-Martorell |
| pt | Síndrome angio-osteo-hipotrófico | Síndrome de Servelle-Martorell |
| pl | Zespół naczyniowo-osteohipotroficzny | Zespół Servelle'a i Martorella |
| cs | Angioosteohypotrofický syndrom | Flebektatická osteohypoplastická angiodysplázie · Servellův-Martorellův syndrom · Servelle-Martorellův syndrom |
| uk | Ангіоостеогіпотрофічний синдром | Флебектатична остеогіпопластична ангіодисплазія · Синдром Сервеля-Мартореля |
| zh | 血管骨营养不良综合征 | 血管骨营养不良综合征 |
| tr | Anjiyoosteohipotrofik sendrom | Servelle-Martorell sendromu · Flebektatik osteohipoplastik anjiyodisplazi |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019156 | E | validated | |
| UMLS | C4707561 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/75508
- This record as JSON: /data/d/75508.json